Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.

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01 1Nuray Chemicals Private Limited
02 1Biophore India Pharmaceuticals Pvt Ltd
03 1Cohance Lifesciences
04 1HRV Pharma
05 1Shamrock Pharmachemi
06 1Curia
07 1Actavis Inc
08 1Apicore
09 1Apino Pharma
10 2Apothecon Pharmaceuticals
11 1Azico Biophore India Pvt. Ltd
12 1BrightGene Bio-Medical Technology Co.,Ltd
13 1Dasami Lab
14 1Emcure Pharmaceuticals
15 2MSN Laboratories
16 1ORGANICA Feinchemie GmbH Wolfen
17 1Optimus Pharma
18 1Piramal Pharma Solutions
19 1Prajna Generics
20 1SKVen Technologies Pvt. Ltd
21 1Sumitomo Chemical
22 1Suven Life Sciences Limited
23 1Viatris
24 1Blank
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01 2China
02 1Germany
03 17India
04 1Ireland
05 1Japan
06 3U.S.A
07 1Blank
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01 9Active
02 3Inactive
03 14Blank
01 26Blank
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01 1218MF10740
02 25Blank
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01 1WC-0042N
02 1WC-0226
03 1WC-0281
04 1WC-0369
05 1WC-0369n
06 1WC-0404
07 1WC-0416
08 19Blank
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01 26Blank
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01 114593-914
02 150379-0017
03 150379-0025
04 158159-031
05 159285-026
06 165392-2901
07 168022-7052
08 169575-4003
09 170966-0016
10 176339-133
11 16Blank
01 26Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-12-23
Pay. Date : 2016-09-13
DMF Number : 30878
Submission : 2016-11-08
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
NDC Package Code : 58159-031
Start Marketing Date : 2024-12-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-03-01
Pay. Date : 2015-09-15
DMF Number : 29527
Submission : 2015-09-03
Status : Active
Type : II
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Curia- A partner for the pharma and biotech industries to improve patient outcomes & quality of life.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-21
Pay. Date : 2014-05-07
DMF Number : 12659
Submission : 1997-09-18
Status : Active
Type : II
NDC Package Code : 65392-2901
Start Marketing Date : 1985-11-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-09-03
Pay. Date : 2018-07-17
DMF Number : 32956
Submission : 2018-07-19
Status : Active
Type : II
Date of Issue : 2022-08-16
Valid Till : 2025-07-15
Written Confirmation Number : WC-0042N
Address of the Firm :

GDUFA
DMF Review : Reviewed
Rev. Date : 2020-10-23
Pay. Date : 2020-06-19
DMF Number : 34910
Submission : 2020-08-28
Status : Active
Type : II
NDC Package Code : 70966-0016
Start Marketing Date : 1985-11-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5351
Submission : 1984-05-17
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32113
Submission : 2017-12-13
Status : Inactive
Type : II

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PharmaCompass offers a list of Trientine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Trientine Hydrochloride manufacturer or Trientine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Trientine Hydrochloride API Price utilized in the formulation of products. Trientine Hydrochloride API Price is not always fixed or binding as the Trientine Hydrochloride Price is obtained through a variety of data sources. The Trientine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trien manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trien, including repackagers and relabelers. The FDA regulates Trien manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trien API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Trien supplier is an individual or a company that provides Trien active pharmaceutical ingredient (API) or Trien finished formulations upon request. The Trien suppliers may include Trien API manufacturers, exporters, distributors and traders.
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We have 23 companies offering Trien
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